Pharmaceutical Books

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• Packaging Details: Set of 4 Books

Approx. Rs 63,000 / SetGet Latest Price

The Japanese Pharmacopoeia is the pharmaceutical standard that the Japanese Minister of Health, Labour and Welfare (MHLW) establishes to regulate the properties and quality of drugs.

As with other pharmacopoeias, the document is revised periodically. The 18th edition (JP18) came into effect on June 7, 2021. The text is originally prepared in Japanese and translated to English after the publication of the Japanese version. This usually is done within one year. According to the publication schedule, Supplement I to JP18 is to be published in December 2022 and Supplement II in 2024. It is planned that the 19th edition will be published in 2026.

_{Content of JP18 English Version}

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Approx. Rs 49,500 / SetGet Latest Price

Available to order from July 2022 / Effective from 1 January 2023

The European Pharmacopoeia (Ph. Eur.) is the primary source of official quality standards for medicines and their ingredients in Europe. Ph. Eur. standards provide a scientic basis for the quality control of a product throughout its life cycle, supporting the pharmaceutical industry and healthcare systems.

As laid down in the Council of Europe Convention on the Elaboration of a European Pharmacopoeia and in European Union and national pharmaceutical legislation, these standards are legally binding. They become mandatory on the same date in all states parties to the convention.

•  New edition, legally binding in 39 European countries as of 1 January 2023 and applied in more than 130 countries worldwide.
• Continually updated and modernised to meet users'''' needs. 
• The 11th Edition of the Ph. Eur. contains:
  • 2 469 monographs (including dosage forms);
  • 386 general texts (including general monographs and methods of analysis);
  • and more than 2 800 descriptions of reagents.
• Released in July 2022 and will be updated with eight periodic supplements over the following three years (11.1 to 11.8).

• three initial volumes (11.0), followed by eight non-cumulative supplements (11.1 to 11.8);
• available in either English or French;
• now with QR codes for easier linking to the Knowledge database for each monograph and general chapter;
• contains a subscription key (EPID code) giving access to the Ph. Eur. online archives.

Note that the 11th Edition print version will no longer contain change marks in revised and corrected texts.

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Approx. Rs 8,000 / BookGet Latest Price

• Amended extracts from the Human Medicines Regulations 2012 relating to:
• manufacture, importation and assembly
• wholesale dealing
• brokering medicine
• manufacturing, importing and distributing active substances

• The Code of Practice for Qualified Persons, Guidance on Manufacture and Importation
• UK guidance on complying with the EU guidelines on Good Distribution Practice for wholesale distributors and brokers of medicines and manufacturers, importers and distributors or active substances
• UK guidance on: risk-based inspections, conditions of holding a manufacturer’s licence, wholesale dealer’s licence, a broker registration and an active substance registration, and controls on certain medicinal products.

• conditions of holding a manufacturing authorisation for investigational medicinal products,
• importing guidance for investigational medicinal products from countries on a list to Great Britain,
• Pharmaceutical Quality System expectations and Authorisation requirements for investigational medicinal products importation oversight,
• list of approved countries for import,
• pharmacovigilance for wholesalers,
• the naming of sites on a wholesale dealer’s licence,
• self-inspection for wholesale dealers and the responsible person for import.

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Approx. Rs 1 Lakh / PackGet Latest Price

System Requirements:

• One free USB 2.0 slot.
• Close any screen capture program (e.g., SnagIT, Adobe Photoshop, Snipping Tool) currently open.

Operating Systems:

• Windows only – XP and above

USP is aware of minor technical issues with the USP-NF English and Spanish USB drive format products. These issues are rare and most appear to be limited to systems running Windows 10. If you experience an "Access violation" error message while using the search function, please close the Lock Lizard application and restart. If you experience any other problems, please submit the webform.

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Approx. Rs 93,600 / SetGet Latest Price

Updated annually, the British Pharmacopoeia (BP) is the only comprehensive collection of authoritative official standards for UK pharmaceutical substances and medicinal products.

It includes approximately 4,000 monographs which are legally enforced by the Human Medicines Regulations 2012. Where a BP monograph exists, medicinal products or active pharmaceutical ingredients sold or supplied in the UK must comply with the relevant monograph.

All monographs and requirements of the European Pharmacopoeia (Ph. Eur.) are reproduced in the BP, making the BP a convenient and fully comprehensive set of standards that can be used across Europe and beyond.

The BP 2023 supersedes the BP 2022 and becomes legally effective on 1 January 2023. This edition incorporates new monographs from both the BP and Ph. Eur. along with a significant number of revised monographs.

• 23 new BP monographs, 59 new Ph. Eur. monographs.
• 151 amended BP monographs.
• All monographs from the Ph. Eur. 10th edition as amended by Supplements 10.1 to 10.8 are included.
• Ph. Eur. supplements 11.0, 11.1, and 11.2 included as in-year online and download product updates.

Ensure you get the best value access to the information you need. Choose from a range of flexible licences and formats - including full online and offline access.

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